Uromed Corp.
United StatesFDA applicant, unverified
- Devices
- 11
What Uromed Corp. makes
Uromed Corp. manufactures surgical aids and devices for urological procedures, including the CaverMap surgical aid for penile vascular mapping and its modified versions, as well as the Uromed Needle Grasper for precise tissue handling. The company also produces urinary control solutions such as the Uromed Patch, Uromed Sling Kit, and the Reliance Urinary Control Insert & Sizing Device for continence management. Additionally, it supplies brachytherapy sources like Iodine-125 implants for targeted radiation therapy and a nerve stimulator for urological applications.
The company’s portfolio includes devices classified under FDA categories Class I, Class II, and Class III, with regulatory submissions documented via 510(k) and PMA pathways. These products are listed in the FDA’s regulatory databases, and the manufacturer operates from the United States.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Uromed Corp. have in the registry?
The registry currently lists 11 devices for Uromed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uromed Corp.'s devices?
Among its 11 most recently registered devices, Uromed Corp. has devices listed in FDA 510(k) (10 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Uromed Corp.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Uromed Corp.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Uromed Corp. in the registry?
The most recently registered devices listed for Uromed Corp. include UROMED PATCH, MODIFICATION TO CAVERMAP SURGICAL AID, UROMED NEEDLE GRASPER and CAVERMAP SURGICAL AID.